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The safety evaluation of food flavoring substances: the role of genotoxicity studies.
Gooderham, Nigel J; Cohen, Samuel M; Eisenbrand, Gerhard; Fukushima, Shoji; Guengerich, F Peter; Hecht, Stephen S; Rietjens, Ivonne M C M; Rosol, Thomas J; Bastaki, Maria; Linman, Matthew J; Taylor, Sean V.
Afiliação
  • Gooderham NJ; Department of Surgery and Cancer, Imperial College, London, UK.
  • Cohen SM; Havlik-Wall Professor of Oncology, Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, USA.
  • Eisenbrand G; Food Chemistry & Toxicology, University of Kaiserslautern (retired), Heidelberg, Germany.
  • Fukushima S; Japan Bioassay Research Center, Kanagawa, Japan.
  • Guengerich FP; Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN, USA.
  • Hecht SS; Masonic Cancer Center and Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
  • Rietjens IMCM; Division of Toxicology, Wageningen University, Wageningen, The Netherlands.
  • Rosol TJ; Department of Biomedical Sciences, Heritage College of Osteopathic Medicine, Ohio University, Athens, OH, USA.
  • Bastaki M; Flavor and Extract Manufacturers Association, Washington, DC, USA.
  • Linman MJ; Flavor and Extract Manufacturers Association, Washington, DC, USA.
  • Taylor SV; Flavor and Extract Manufacturers Association, Washington, DC, USA.
Crit Rev Toxicol ; 50(1): 1-27, 2020 01.
Article em En | MEDLINE | ID: mdl-32162576
ABSTRACT
The Flavor and Extract Manufacturers Association (FEMA) Expert Panel relies on the weight of evidence from all available data in the safety evaluation of flavoring substances. This process includes data from genotoxicity studies designed to assess the potential of a chemical agent to react with DNA or otherwise cause changes to DNA, either in vitro or in vivo. The Panel has reviewed a large number of in vitro and in vivo genotoxicity studies during the course of its ongoing safety evaluations of flavorings. The adherence of genotoxicity studies to standardized protocols and guidelines, the biological relevance of the results from those studies, and the human relevance of these studies are all important considerations in assessing whether the results raise specific concerns for genotoxic potential. The Panel evaluates genotoxicity studies not only for evidence of genotoxicity hazard, but also for the probability of risk to the consumer in the context of exposure from their use as flavoring substances. The majority of flavoring substances have given no indication of genotoxic potential in studies evaluated by the FEMA Expert Panel. Examples illustrating the assessment of genotoxicity data for flavoring substances and the consideration of the factors noted above are provided. The weight of evidence approach adopted by the FEMA Expert Panel leads to a rational assessment of risk associated with consumer intake of flavoring substances under the conditions of use.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aromatizantes / Testes de Mutagenicidade Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Crit Rev Toxicol Assunto da revista: TOXICOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Aromatizantes / Testes de Mutagenicidade Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Crit Rev Toxicol Assunto da revista: TOXICOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido